首页> 外文期刊>European journal of pharmaceutical sciences >Preparation and evaluation of clindamycin phosphate loaded chitosan/alginate polyelectrolyte complex film as mucoadhesive drug delivery system for periodontal therapy
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Preparation and evaluation of clindamycin phosphate loaded chitosan/alginate polyelectrolyte complex film as mucoadhesive drug delivery system for periodontal therapy

机译:Clindamycin磷酸盐的制备和评估壳聚糖/藻酸盐聚电解质复合膜作为牙周治疗的粘膜粘附药物递送系统

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摘要

In this study, Clindamycin phosphate loaded adhesive polyelectrolyte complex films for local periodontal therapy were prepared with alginate and chitosan. The thickness, drug content, structure, swelling, adhesion and in vitro drug release with release kinetics of formulations were evaluated. The effects of the varying concentration and molecular weight of polymers used and the volume of the polymer solutions on the characteristics of the films were investigated. Increasing the concentration of sodium alginate in total content of polymer mixture caused to higher adhesiveness. Chitosan molecular weight also affected to adhesiveness of complex films. The release rate of drug and release kinetics was affected from the complexation. The best complexation was obtained with the three times higher concentration and volume of alginate in combination with low molecular weight chitosan. Thus polyelectrolyte films that have delayed release together with high swelling ability and adhesiveness and high drug content were formed. Due to the heterogeneous structure of complex film, the release profiles of the formulations fitted to the anomalous transport mechanism. 3D structure of the drug loaded complex film was analyzed by Micro-CT imaging in this study and it was showed that using this method would be very advantageous for further studies about the investigation of complexation than the other imaging methods in order to determine the volume and the size of the formed complexes within the structure at the same time.
机译:在该研究中,用藻酸盐和壳聚糖制备用于局部牙周治疗的Clindamycin磷酸粘接粘合剂聚电解质复合膜。评价厚度,药物含量,结构,溶胀,附着力和体外药物释放,具有制剂的释放动力学。研究了所使用的聚合物的不同浓度和分子量的影响和聚合物溶液的体积对薄膜的特性。增加了聚合物混合物总含量的藻酸钠浓度,使其较高的粘合性。壳聚糖分子量也受复合膜的粘合性。药物和释放动力学的释放率受到络合的影响。用低分子量壳聚糖组合的浓度高出浓度和藻酸盐体积的三倍,得到了最佳络合。因此,形成具有延迟释放以及高溶胀能力和粘合性和高药物含量的聚电解质薄膜。由于复合膜的异质结构,配方的释放曲线适用于异常输送机制。通过该研究的微型CT成像分析了药物负载复杂膜的3D结构,并且表明使用该方法对于进一步研究络合的研究比其他成像方法来说是非常有利的,以便确定体积和同时结构内形成的复合物的尺寸。

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